Human Phenotype Ontology 
Grandparent Node:
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Congenital malformation of the right heart (HP:0011723)help
Grandparent Node:
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Conotruncal defect (HP:0001710)help
Parent Node:
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Double outlet right ventricle (HP:0001719)help
..Starting node
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Double outlet right ventricle with subaortic ventricular septal defect without pulmonary stenosis (HP:0011656)help
Term ID: 11656
Name: Double outlet right ventricle with subaortic ventricular septal defect without pulmonary stenosis
Synonym: DORV with subaortic VSD without pulmonary stenosis
Definition: A double outlet right ventricle with a ventricular spetal defect (a hole between the two bottom chambers (ventricles) of the heart), that is considered to be closely related to the aortic origin. There is not associated pulmonary stenosis, the abnormal narrowing or constriction of the pulmonary artery, in the main pulmonary artery and/or in the left or right pulmonary artery branches.
Comments:
Reference: HP:0011656
Genes and Diseases:
 
       Child Nodes:

 Sister Nodes: 
..expandDouble outlet right ventricle with doubly committed ventricular septal defect and pulmonary stenosis (HP:0011651) help
..expandDouble outlet right ventricle with doubly committed ventricular septal defect without pulmonary stenosis (HP:0011652) help
..expandDouble outlet right ventricle with non-committed ventricular septal defect and pulmonary stenosis (HP:0011653) help
..expandDouble outlet right ventricle with non-committed ventricular septal defect without pulmonary stenosis (HP:0011654) help
..expandDouble outlet right ventricle with subaortic ventricular septal defect and pulmonary stenosis (HP:0011655) help
..expandDouble outlet right ventricle with subpulmonary ventricular septal defect and pulmonary stenosis (HP:0011657) help
..expandDouble outlet right ventricle with subpulmonary ventricular septal defect without pulmonary stenosis (HP:0011658) help
InputHPO IDHPO termDistanceGeneGene id entrezHGNC IDDiseaseIdDiseaseNameFrequencyOnsetHGMD variantsClinVar variants
 
HPO disease - gene - phenotype typical associations:
 
HPO disease - gene - phenotype less frequent non-typical associations:
HP:0011656HP:0011656Double outlet right ventricle with subaortic ventricular septal defect without pulmonary stenosis0 CL E G H


Genes (0) :

Diseases (0) :
 

Human Phenotype Ontology(HPO) is developed by the Human Phenotype Ontology Consortium. The version used here is December 15 2022 release.